Elimination of replication block protein Fob1 extends the life span of yeast mother cells

被引:323
作者
Defossez, PA
Prusty, R
Kaeberlein, M
Lin, SJ
Ferrigno, P
Silver, PA
Keil, RL
Guarente, L
机构
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
[2] Penn State Univ, Milton S Hershey Med Ctr, Dept Biochem & Mol Biol, Hershey, PA 17033 USA
[3] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1097-2765(00)80472-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A cause of aging in yeast is the accumulation of circular species of ribosomal DNA (rDNA) arising from the 100-200 tandemly repeated copies in the genome. We show here that mutation of the FOB1 gene slows the generation of these circles and thus extends life span. Fob1p is known to create a unidirectional block to replication forks in the rDNA. We show that Fob1p is a nucleolar protein, suggesting a direct involvement in the replication fork block. We propose that this block can trigger aging by causing chromosomal breaks, the repair of which results in the generation of rDNA circles. These findings may provide a novel link between metabolic rate and aging in yeast and, perhaps, higher organisms.
引用
收藏
页码:447 / 455
页数:9
相关论文
共 49 条
[41]   Loss of transcriptional silencing causes sterility in old mother cells of S-cerevisiae [J].
Smeal, T ;
Claus, J ;
Kennedy, B ;
Cole, F ;
Guarente, L .
CELL, 1996, 84 (04) :633-642
[42]   LOSS OF HYBRIDIZABLE RIBOSOMAL DNA FROM HUMAN POST-MITOTIC TISSUES DURING AGING .1. AGE-DEPENDENT LOSS IN HUMAN MYOCARDIUM [J].
STREHLER, BL ;
CHANG, MP ;
JOHNSON, LK .
MECHANISMS OF AGEING AND DEVELOPMENT, 1979, 11 (5-6) :371-378
[43]   RECOMBINATION-STIMULATING SEQUENCES IN YEAST RIBOSOMAL DNA CORRESPOND TO SEQUENCES REGULATING TRANSCRIPTION BY RNA POLYMERASE-I [J].
VOELKELMEIMAN, K ;
KEIL, RL ;
ROEDER, GS .
CELL, 1987, 48 (06) :1071-1079
[44]  
WACH A, 1994, YEAST, V10, P1773
[45]   SGS1 - A EUKARYOTIC HOMOLOG OF ESCHERICHIA-COLI RECQ THAT INTERACTS WITH TOPOISOMERASE-II IN-VIVO AND IS REQUIRED FOR FAITHFUL CHROMOSOME SEGREGATION [J].
WATT, PM ;
LOUIS, EJ ;
BORTS, RH ;
HICKSON, ID .
CELL, 1995, 81 (02) :253-260
[46]   Caloric intake and aging [J].
Weindruch, R ;
Sohal, RS .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (14) :986-994
[47]   REPLICATION FORK BARRIERS IN THE XENOPUS RDNA [J].
WIESENDANGER, B ;
LUCCHINI, R ;
KOLLER, T ;
SOGO, JM .
NUCLEIC ACIDS RESEARCH, 1994, 22 (23) :5038-5046
[48]   Replication focus-forming activity 1 and the Werner syndrome gene product [J].
Yan, H ;
Chen, CY ;
Kobayashi, R ;
Newport, J .
NATURE GENETICS, 1998, 19 (04) :375-378
[49]   Holliday junctions accumulate in replication mutants via a RecA homolog-independent mechanism [J].
Zou, H ;
Rothstein, R .
CELL, 1997, 90 (01) :87-96